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Study Management

Study Management

Managed Programs

Stud Management Team
  • Worker / Operator Safety

  • Environmental Safety / Air Monitoring

    • Field Volatility

    • Flux

  • Dislodgeable Foliar Residue

  • Turf Transferable Residue

  • Field Efficacy Programs

    • Herbicide

    • Insecticide

    • Fungicide

    • PGR

    • Bio-stimulants

Study Management Team

Fred Rice

Study Director - E-fate, Residue, Pollinator, Volatility/Flux

M.S. Plant Physiology / Biochemistry - University of Missouri / Columbia

Fred@LangeRC.com

Alex Gibbs 

Study Director - E-fate, Pollinator, Volatility/Flux

B.S. Plant Science -University of Missouri / Columbia

Alex@LangeRC.com

Andrew (Andy) Thiel 

Study Director - Residue E-fate

B.S. Plant Science -University of Missouri / Columbia

Andrew@LangeRC.com

Ali Csinos

Study Director - Residue, Efficacy

Ali@LangeRC.com

Environmental Fate Studies

PM E-Fate Studies
  • Over 80 years of combined experience

  • Managed over 400 environmental fate studies

 

  • Regular sponsor communication

  • Confirmation of application rates and sampling dates

  • Track shipments to the laboratory

 

  • Site instrumentation

  • California irrigation requirements

  • Soil moisture and evapo-transpiration data

  • Accurate application of water inputs.

  • On-site for study kickoff

PM Pollinator Studies

Pollinator Studies

  • Managed over 80 pollinator related studies

  • Estimated 150 locations in the US, Columbia, and Brazil

 

  • Pollen and nectar collection

  • Semi-field

  • Hive feeding studies

 

  • Ensure consistent sampling techniques

  • Supply written sampling instructions for PFI

  • Supply all sampling containers

  • Practice sampling techniques ahead of time

  • On-site for the first sampling event for training  

PM Mag Res Studies

Magnitude of the Residue Studies

  • Managed over 600 residue study programs

  • Placed over 6,000 trials across the US, as well as Central and South America.  

  • Regular sponsor communication

  • Confirmation of application rates and sampling dates

  • Track shipments to the laboratory

  • Start the reporting process at the time of the first application

  • Establishment timelines early in the study

  • Monitor progress of sample analysis

  • Meet sponsor reporting timeline    

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